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FURTHER STUDY OF SOMA DENDRITE AND AXON EXCITATION IN SINGLE NEURONS

机译:单神经元中SOMA树突和轴突激发的进一步研究

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摘要

The present investigation continues a previous study in which the soma-dendrite system of sensory neurons was excited by stretch deformation of the peripheral dendrite portions. Recording was done with intracellular leads which were inserted into the cell soma while the neuron was activated orthodromically or antidromically. The analysis was also extended to axon conduction. Crayfish, Procambarus alleni (Faxon) and Orconectes virilis (Hagen), were used. 1. The size and time course of action potentials recorded from the soma-dendrite complex vary greatly with the level of the cell's membrane potential. The latter can be changed over a wide range by stretch deformation which sets up a "generator potential" in the distal portions of the dendrites. If a cell is at its resting unstretched equilibrium potential, antidromic stimulation through the axon causes an impulse which normally overshoots the resting potential and decays into an afternegativity of 15 to 20 msec. duration. The postspike negativity is not followed by an appreciable hyperpolarization (positive) phase. If the membrane potential is reduced to a new steady level a postspike positivity appears and increases linearly over a depolarization range of 12 to 20 mv. in various cells. At those levels the firing threshold of the cell for orthodromic discharges is generally reached. 2. The safety factor for conduction between axon and cell soma is reduced under three unrelated conditions, (a) During the recovery period (2 to 3 msec.) immediately following an impulse which has conducted fully over the cell soma, a second impulse may be delayed, may invade the soma partially, or may be blocked completely. (b) If progressive depolarization is produced by stretch, it leads to a reduction of impulse height and eventually to complete block of antidromic soma invasion, resembling cathodal block, (c) In some cells, when the normal membrane potential is within several millivolts of the relaxed resting state, an antidromic impulse may be blocked and may set up within the soma a local potential only. The local potential can sum with a second one or it may sum with potential changes set up in the dendrites, leading to complete invasion of the soma. Such antidromic invasion block can always be relieved by appropriate stretch which shifts the membrane potential out of the "blocking range" nearer to the soma firing level. During the afterpositivity of an impulse in a stretched cell the membrane potential may fall below or near the blocking range. During that period another impulse may be delayed or blocked. 3. Information regarding activity and conduction in dendrites has been obtained indirectly, mainly by analyzing the generator action under various conditions of stretch. The following conclusions have been reached: The large dendrite branches have similar properties to the cell body from which they arise and carry the same kind of impulses. In the finer distal filaments of even lightly depolarized dendrites, however, no axon type all-or-none conduction occurs since the generator potential persists to a varying degree during antidromic invasion of the cell. With the membrane potential at its resting level the dendrite terminals contribute to the prolonged impulse afternegativity of the soma. 4. Action potentials in impaled axons and in cell bodies have been compared. It is thought that normally the over-all duration of axon impulses is shorter. Local activity during reduction of the safety margin for conduction was studied. 5. An analysis was made of high frequency grouped discharges which occasionally arise in cells. They differ in many essential aspects from the regular discharges set up by the generator action. It is proposed that grouped discharges occur only when invasion of dendrites is not synchronous, due to a delay in excitation spread between soma and dendrites. Each impulse in a group is assumed to be caused by an impulse in at least one of the large dendrite branches. Depolarization of dendrites abolishes the grouped activity by facilitating invasion of the large dendrite branches.
机译:本研究继续了先前的研究,其中感觉神经元的体-树突系统通过外围树突部分的拉伸变形而被激发。记录是通过将细胞内导线插入细胞体中进行的,而神经元则是通过正射或反射被激活的。该分析还扩展到轴突传导。使用了小龙虾,Procambarus alleni(Faxon)和Viconis virilis(Hagen)。 1.从体-树突状复合体记录的动作电位的大小和时间过程随细胞膜电位的水平而变化很大。后者可以通过拉伸变形而在很宽的范围内变化,该拉伸变形在树枝状晶体的远端部分建立了“发电机电位”。如果细胞处于其静止的未拉伸平衡电位,则通过轴突的反皮肤刺激会产生脉冲,该脉冲通常会超过静止电位,并衰减为15到20毫秒的负负性。持续时间。峰后负性之后没有明显的超极化(正)阶段。如果膜电位降低到新的稳定水平,则在12至20 mv的去极化范围内会出现刺后阳性,并呈线性增加。在各种细胞中。在那些水平上,通常达到用于正畸放电的电池的点火阈值。 2.在三种不相关的条件下,轴突和细胞体之间传导的安全系数降低了:(a)在完全对细胞体进行传导的冲动之后的恢复期(2至3毫秒)内,可能会有第二次冲动延迟,可能部分侵入躯体或完全被阻塞。 (b)如果通过拉伸产生进行性去极化,则会导致冲动高度降低,并最终完成抗体细胞侵入的阻滞,类似于阴极阻滞;(c)在某些细胞中,正常膜电位在几毫伏的范围内。在放松的静息状态下,可能会阻止抗躯体冲动,并可能在躯体内建立局部电位。局部电势可以与第二电势相加,也可以与树突中建立的电势变化相加,从而导致对躯体的完全入侵。始终可以通过适当的拉伸来缓解这种抗蠕虫的侵袭,该拉伸将膜电位移至更接近于躯体发射水平的“阻滞范围”之外。在拉伸细胞中冲动的后阳性过程中,膜电位可能会低于或接近阻断范围。在此期间,另一种冲动可能会延迟或阻止。 3.主要通过分析在各种拉伸条件下的生成器作用,间接获得有关树突中活性和传导的信息。已经得出以下结论:大的树枝状树枝具有与其产生的细胞体相似的特性,并带有相同种类的脉冲。然而,在甚至极去极化的树突的较细的远端细丝中,由于在细胞的反线侵入过程中发生器电位在不同程度上持续存在,所以没有轴突型全或无传导发生。膜电位处于静止状态时,枝晶末端有助于延长躯体的脉冲后负性。 4.已经比较了刺破的轴突和细胞体内的动作电位。通常认为轴突脉冲的总持续时间较短。研究了降低传导安全裕度期间的局部活动。 5.对高频分组放电进行了分析,这种放电有时会在电池中产生。它们在许多重要方面与发电机动作产生的常规放电不同。有人提出,由于体细胞和树突之间的激发扩散延迟,只有在树突的侵入不同步时才发生分组放电。假定一组中的每个脉冲是由至少一个大的树枝状分支中的脉冲引起的。树突的去极化通过促进大树突分支的入侵而消除了成群的活动。

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